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The Journal of Molecular Diagnostics : JMD
|
May 3, 2002
Diagnosis of five spinocerebellar ataxia disorders by multiplex amplification and capillary electrophoresis
Michael O Dorschner, Deborah Barden, Karen Stephens
Genes, Chromosomes & Cancer
|
July 6, 2004
Genomic context of paralogous recombination hotspots mediating recurrent NF1 region microdeletion
Stephen H Forbes, Michael O Dorschner, Rosalynda Le, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 26, 2014
Regulatory changes raise troubling questions for genomic testing
Barbara J Evans, Michael O Dorschner, Wylie Burke, et al.
Journal of Genetic Counseling
|
January 4, 2021
Genetic counseling for early onset and familial dementia: Patient perspectives on exome sequencing
Bradley Rolf, Elizabeth E Blue, Stephanie Bucks, et al.
Genes & Development
|
February 20, 2008
Oct4 dependence of chromatin structure within the extended Nanog locus in ES cells
Dana N Levasseur, Jianlong Wang, Michael O Dorschner, et al.
Genes, Chromosomes & Cancer
|
April 16, 2003
Complete physical map and gene content of the human NF1 tumor suppressor region in human and mouse
Dieter E Jenne, Sigrid Tinschert, Michael O Dorschner, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation
|
December 17, 2017
LMX1B-Associated Nephropathy With Type III Collagen Deposition in the Glomerular and Tubular Basement Membranes
Nicole K Andeen, Jennifer Schleit, Christopher D Blosser, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 9, 2004
Genome-wide identification of DNaseI hypersensitive sites using active chromatin sequence libraries
Peter J Sabo, Richard Humbert, Michael Hawrylycz, et al.
Human Gene Therapy
|
October 11, 2011
Gammaretroviral vector integration occurs overwhelmingly within and near DNase hypersensitive sites
Mingdong Liu, Chang Long Li, George Stamatoyannopoulos, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
March 6, 2015
Development of clinical decision support alerts for pharmacogenomic incidental findings from exome sequencing
Adam A Nishimura, Brian H Shirts, Michael O Dorschner, et al.
Page
of 7
Search research articles
Search
Showing results (1-10 of 66) with videos related to
Sort By:
Page
of 7
The Journal of Molecular Diagnostics : JMD
|
May 3, 2002
Diagnosis of five spinocerebellar ataxia disorders by multiplex amplification and capillary electrophoresis
Michael O Dorschner, Deborah Barden, Karen Stephens
Genes, Chromosomes & Cancer
|
July 6, 2004
Genomic context of paralogous recombination hotspots mediating recurrent NF1 region microdeletion
Stephen H Forbes, Michael O Dorschner, Rosalynda Le, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 26, 2014
Regulatory changes raise troubling questions for genomic testing
Barbara J Evans, Michael O Dorschner, Wylie Burke, et al.
Journal of Genetic Counseling
|
January 4, 2021
Genetic counseling for early onset and familial dementia: Patient perspectives on exome sequencing
Bradley Rolf, Elizabeth E Blue, Stephanie Bucks, et al.
Genes & Development
|
February 20, 2008
Oct4 dependence of chromatin structure within the extended Nanog locus in ES cells
Dana N Levasseur, Jianlong Wang, Michael O Dorschner, et al.
Genes, Chromosomes & Cancer
|
April 16, 2003
Complete physical map and gene content of the human NF1 tumor suppressor region in human and mouse
Dieter E Jenne, Sigrid Tinschert, Michael O Dorschner, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation
|
December 17, 2017
LMX1B-Associated Nephropathy With Type III Collagen Deposition in the Glomerular and Tubular Basement Membranes
Nicole K Andeen, Jennifer Schleit, Christopher D Blosser, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 9, 2004
Genome-wide identification of DNaseI hypersensitive sites using active chromatin sequence libraries
Peter J Sabo, Richard Humbert, Michael Hawrylycz, et al.
Human Gene Therapy
|
October 11, 2011
Gammaretroviral vector integration occurs overwhelmingly within and near DNase hypersensitive sites
Mingdong Liu, Chang Long Li, George Stamatoyannopoulos, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
March 6, 2015
Development of clinical decision support alerts for pharmacogenomic incidental findings from exome sequencing
Adam A Nishimura, Brian H Shirts, Michael O Dorschner, et al.
Page
of 7